Temporal Gradients Controlling Embryonic Cell Cycle
Cell proliferation in early embryos by rapid cell cycles and its abrupt pause after a stereotypic number of divisions present an attractive system to study the timing mechanism in general and its coordination with developmental progression. In animals with large eggs, such as <i>Xenopus</i&...
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doaj-9fff213bb85f4a90acb510fa89bb17c02021-06-30T23:44:09ZengMDPI AGBiology2079-77372021-06-011051351310.3390/biology10060513Temporal Gradients Controlling Embryonic Cell CycleBoyang Liu0Han Zhao1Keliang Wu2Jörg Großhans3Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan 250012, ChinaCenter for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan 250012, ChinaCenter for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan 250012, ChinaDepartment of Biology, Philipps University, 35043 Marburg, GermanyCell proliferation in early embryos by rapid cell cycles and its abrupt pause after a stereotypic number of divisions present an attractive system to study the timing mechanism in general and its coordination with developmental progression. In animals with large eggs, such as <i>Xenopus</i>, zebrafish, or <i>Drosophila</i>, 11–13 very fast and synchronous cycles are followed by a pause or slowdown of the cell cycle. The stage when the cell cycle is remodeled falls together with changes in cell behavior and activation of the zygotic genome and is often referred to as mid-blastula transition. The number of fast embryonic cell cycles represents a clear and binary readout of timing. Several factors controlling the cell cycle undergo dynamics and gradual changes in activity or concentration and thus may serve as temporal gradients. Recent studies have revealed that the gradual loss of Cdc25 protein, gradual depletion of free deoxyribonucleotide metabolites, or gradual depletion of free histone proteins impinge on Cdk1 activity in a threshold-like manner. In this review, we will highlight with a focus on <i>Drosophila</i> studies our current understanding and recent findings on the generation and readout of these temporal gradients, as well as their position within the regulatory network of the embryonic cell cycle.https://www.mdpi.com/2079-7737/10/6/513embryonic developmentcell cycle remodelingdevelopmental timingmetabolismtemporal gradient |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Boyang Liu Han Zhao Keliang Wu Jörg Großhans |
spellingShingle |
Boyang Liu Han Zhao Keliang Wu Jörg Großhans Temporal Gradients Controlling Embryonic Cell Cycle Biology embryonic development cell cycle remodeling developmental timing metabolism temporal gradient |
author_facet |
Boyang Liu Han Zhao Keliang Wu Jörg Großhans |
author_sort |
Boyang Liu |
title |
Temporal Gradients Controlling Embryonic Cell Cycle |
title_short |
Temporal Gradients Controlling Embryonic Cell Cycle |
title_full |
Temporal Gradients Controlling Embryonic Cell Cycle |
title_fullStr |
Temporal Gradients Controlling Embryonic Cell Cycle |
title_full_unstemmed |
Temporal Gradients Controlling Embryonic Cell Cycle |
title_sort |
temporal gradients controlling embryonic cell cycle |
publisher |
MDPI AG |
series |
Biology |
issn |
2079-7737 |
publishDate |
2021-06-01 |
description |
Cell proliferation in early embryos by rapid cell cycles and its abrupt pause after a stereotypic number of divisions present an attractive system to study the timing mechanism in general and its coordination with developmental progression. In animals with large eggs, such as <i>Xenopus</i>, zebrafish, or <i>Drosophila</i>, 11–13 very fast and synchronous cycles are followed by a pause or slowdown of the cell cycle. The stage when the cell cycle is remodeled falls together with changes in cell behavior and activation of the zygotic genome and is often referred to as mid-blastula transition. The number of fast embryonic cell cycles represents a clear and binary readout of timing. Several factors controlling the cell cycle undergo dynamics and gradual changes in activity or concentration and thus may serve as temporal gradients. Recent studies have revealed that the gradual loss of Cdc25 protein, gradual depletion of free deoxyribonucleotide metabolites, or gradual depletion of free histone proteins impinge on Cdk1 activity in a threshold-like manner. In this review, we will highlight with a focus on <i>Drosophila</i> studies our current understanding and recent findings on the generation and readout of these temporal gradients, as well as their position within the regulatory network of the embryonic cell cycle. |
topic |
embryonic development cell cycle remodeling developmental timing metabolism temporal gradient |
url |
https://www.mdpi.com/2079-7737/10/6/513 |
work_keys_str_mv |
AT boyangliu temporalgradientscontrollingembryoniccellcycle AT hanzhao temporalgradientscontrollingembryoniccellcycle AT keliangwu temporalgradientscontrollingembryoniccellcycle AT jorggroßhans temporalgradientscontrollingembryoniccellcycle |
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1721350574103855104 |